1. Clinical exome sequencing in early‐onset generalized dystonia and large‐scale resequencing follow‐up. Issue 4 (26th September 2016) Authors: Zech, Michael; Boesch, Sylvia; Jochim, Angela; Weber, Sandrina; Meindl, Tobias; Schormair, Barbara; Wieland, Thomas; Lunetta, Christian; Sansone, Valeria; Messner, Michael; Mueller, Joerg; Ceballos‐Baumann, Andres; Strom, Tim M.; Colombo, Roberto; Poewe, Werner; Haslinger, Bernhard; Winkelmann, J... Journal: Movement disorders Issue: Volume 32:Issue 4(2017) Page Start: 549 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Comorbidities, treatment, and pathophysiology in restless legs syndrome. Issue 11 (November 2018) Authors: Trenkwalder, Claudia; Allen, Richard; Högl, Birgit; Clemens, Stefan; Patton, Stephanie; Schormair, Barbara; Winkelmann, Juliane Journal: Lancet neurology Issue: Volume 17:Issue 11(2018) Page Start: 994 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. DYT16 revisited: Exome sequencing identifies PRKRA mutations in a European dystonia family. Issue 12 (20th August 2014) Authors: Zech, Michael; Castrop, Florian; Schormair, Barbara; Jochim, Angela; Wieland, Thomas; Gross, Nadine; Lichtner, Peter; Peters, Annette; Gieger, Christian; Meitinger, Thomas; Strom, Tim M.; Oexle, Konrad; Haslinger, Bernhard; Winkelmann, Juliane Journal: Movement disorders Issue: Volume 29:Issue 12(2014) Page Start: 1504 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. Issue 11 (November 2017) Authors: Schormair, Barbara; Zhao, Chen; Bell, Steven; Tilch, Erik; Salminen, Aaro V; Pütz, Benno; Dauvilliers, Yves; Stefani, Ambra; Högl, Birgit; Poewe, Werner; Kemlink, David; Sonka, Karel; Bachmann, Cornelius G; Paulus, Walter; Trenkwalder, Claudia; Oertel, Wolfgang H; Hornyak, Magdolna; Teder-Laving,... Journal: Lancet neurology Issue: Volume 16:Issue 11(2017:Nov.) Page Start: 898 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. Issue 2 (19th December 2019) Authors: Tilch, Erik; Schormair, Barbara; Zhao, Chen; Salminen, Aaro V.; Antic Nikolic, Ana; Holzknecht, Evi; Högl, Birgit; Poewe, Werner; Bachmann, Cornelius G.; Paulus, Walter; Trenkwalder, Claudia; Oertel, Wolfgang H.; Hornyak, Magdolna; Fietze, Ingo; Berger, Klaus; Lichtner, Peter; Gieger, Christian; ... Journal: Annals of neurology Issue: Volume 87:Issue 2(2020) Page Start: 184 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Iron in Restless Legs Syndrome. Issue 3 (12th June 2014) Authors: Schulte, Eva C.; Kaffe, Maria; Schormair, Barbara; Winkelmann, Juliane Journal: Movement disorders clinical practice Issue: Volume 1:Issue 3(2014) Page Start: 161 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Iron in Restless Legs Syndrome. Issue 3 (12th June 2014) Authors: Schulte, Eva C.; Kaffe, Maria; Schormair, Barbara; Winkelmann, Juliane Journal: Movement disorders clinical practice Issue: Volume 1:Issue 3(2014) Page Start: 161 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease. Issue 7 (14th May 2011) Authors: Schormair, Barbara; Plag, Jens; Kaffe, Maria; Groß, Nadine; Czamara, Darina; Samtleben, Walter; Lichtner, Peter; Ströhle, Andreas; Stefanidis, Ioannis; Vainas, Andreas; Dardiotis, Efthimios; Sakkas, George K; Gieger, Christian; Müller-Myhsok, Bertram; Meitinger, Thomas; Heemann, Uwe; Hadjigeorgio... Journal: Journal of medical genetics Issue: Volume 48:Issue 7(2011) Page Start: 462 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Private variants in PRKN are associated with late-onset Parkinson's disease. (June 2020) Authors: Hopfner, Franziska; Mueller, Stefanie H.; Szymczak, Silke; Junge, Olaf; Tittmann, Lukas; May, Sandra; Lohmann, Katja; Grallert, Harald; Lieb, Wolfgang; Strauch, Konstantin; Müller-Nurasyid, Martina; Berger, Klaus; Schormair, Barbara; Winkelmann, Juliane; Mollenhauer, Brit; Trenkwalder, Claudia; M... Journal: Parkinsonism & related disorders Issue: Volume 75(2020) Page Start: 24 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease. Issue 7 (8th April 2020) Authors: Hopfner, Franziska; Mueller, Stefanie H.; Szymczak, Silke; Junge, Olaf; Tittmann, Lukas; May, Sandra; Lohmann, Katja; Grallert, Harald; Lieb, Wolfgang; Strauch, Konstantin; Müller‐Nurasyid, Martina; Berger, Klaus; Schormair, Barbara; Winkelmann, Juliane; Mollenhauer, Brit; Trenkwalder, Claudia; M... Journal: Movement disorders Issue: Volume 35:Issue 7(2020) Page Start: 1245 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗